196 related articles for article (PubMed ID: 25933678)
1. Identification of a fusion gene composed of a Hippo pathway gene MST2 and a common translocation partner ETV6 in a recurrent translocation t(8;12)(q22;p13) in acute myeloid leukemia.
Ogawa S; Yokoyama Y; Suzukawa K; Nanmoku T; Kurita N; Seki M; Maie K; Suyama T; Takaiwa N; Sakata-Yanagimoto M; Obara N; Hasegawa Y; Chiba S
Ann Hematol; 2015 Aug; 94(8):1431-3. PubMed ID: 25933678
[No Abstract] [Full Text] [Related]
2. Biallelic ETV6 rearrangements by recurrent translocations t(7;12)(p15;p13) and t(3;12)(q26.2;p13) in acute myeloid leukemia.
Yamamoto K; Yakushijin K; Funakoshi Y; Inui Y; Okamura A; Matsuoka H; Minami H
Leuk Res; 2011 Nov; 35(11):e212-4. PubMed ID: 21803420
[No Abstract] [Full Text] [Related]
3. A novel cryptic translocation t(12;17)(p13;p12-p13) in a secondary acute myeloid leukemia results in a fusion of the ETV6 gene and the antisense strand of the PER1 gene.
Murga Penas EM; Cools J; Algenstaedt P; Hinz K; Seeger D; Schafhausen P; Schilling G; Marynen P; Hossfeld DK; Dierlamm J
Genes Chromosomes Cancer; 2003 May; 37(1):79-83. PubMed ID: 12661008
[TBL] [Abstract][Full Text] [Related]
4. A novel t(10;12)(q21;p13) involving ETV6 in a patient with acute myeloid leukemia.
Sowa AS; Meloni-Ehrig AM; Tos A; Jahn J; Dogra S; Nava VE; Kelly JC; Mowrey PN
Cancer Genet Cytogenet; 2010 Dec; 203(2):352-4. PubMed ID: 21156259
[No Abstract] [Full Text] [Related]
5. Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.
Manola KN; Georgakakos VN; Margaritis D; Stavropoulou C; Panos C; Kotsianidis I; Pantelias GE; Sambani C
Cancer Genet Cytogenet; 2008 Jan; 180(1):37-42. PubMed ID: 18068531
[TBL] [Abstract][Full Text] [Related]
6. ETV6-LPXN fusion transcript generated by t(11;12)(q12.1;p13) in a patient with relapsing acute myeloid leukemia with NUP98-HOXA9.
Abe A; Yamamoto Y; Iba S; Kanie T; Okamoto A; Tokuda M; Inaguma Y; Yanada M; Morishima S; Mizuta S; Akatsuka Y; Okamoto M; Kameyama T; Mayeda A; Emi N
Genes Chromosomes Cancer; 2016 Mar; 55(3):242-50. PubMed ID: 26542893
[TBL] [Abstract][Full Text] [Related]
7. Variant of ETV6/ABL1 gene is associated with leukemia phenotype.
Park J; Kim M; Lim J; Kim Y; Han K; Kim JS; Lee S; Kim HJ; Min WS
Acta Haematol; 2013; 129(2):78-82. PubMed ID: 23171811
[TBL] [Abstract][Full Text] [Related]
8. Heterogeneity of the 7q36 breakpoints in the t(7;12) involving ETV6 in infant leukemia.
Tosi S; Hughes J; Scherer SW; Nakabayashi K; Harbott J; Haas OA; Cazzaniga G; Biondi A; Kempski H; Kearney L
Genes Chromosomes Cancer; 2003 Oct; 38(2):191-200. PubMed ID: 12939747
[TBL] [Abstract][Full Text] [Related]
9. ETV6/GOT1 fusion in a case of t(10;12)(q24;p13)-positive myelodysplastic syndrome.
Struski S; Mauvieux L; Gervais C; Hélias C; Liu KL; Lessard M
Haematologica; 2008 Mar; 93(3):467-8. PubMed ID: 18310541
[TBL] [Abstract][Full Text] [Related]
10. Coexpression of ETV6/MDS1/EVI1 and ETV6/EVI1 fusion transcripts in acute myeloid leukemia with t(3;12)(q26.2;p13) and thrombocytosis.
Yamamoto K; Yakushijin K; Ichikawa H; Okamura A; Nagao S; Kakiuchi S; Kurata K; Kawamoto S; Matsui K; Nakamachi Y; Saegusa J; Matsuoka H; Minami H
Leuk Lymphoma; 2019 May; 60(5):1294-1298. PubMed ID: 30526151
[No Abstract] [Full Text] [Related]
11. A Rare Case of ETV6/MECOM Rearrangement in Therapy-Related Acute Myeloid Leukemia with t(3;12) and Monosomy 7.
Kim YJ; Yang JJ; Han Y; Kim S; Yang HS; Yoon HJ; Lee JH; Lee WI; Park TS
Clin Lab; 2017 Feb; 63(2):415-418. PubMed ID: 28182364
[No Abstract] [Full Text] [Related]
12. Identification of a SRC-like tyrosine kinase gene, FRK, fused with ETV6 in a patient with acute myelogenous leukemia carrying a t(6;12)(q21;p13) translocation.
Hosoya N; Qiao Y; Hangaishi A; Wang L; Nannya Y; Sanada M; Kurokawa M; Chiba S; Hirai H; Ogawa S
Genes Chromosomes Cancer; 2005 Mar; 42(3):269-79. PubMed ID: 15611931
[TBL] [Abstract][Full Text] [Related]
13. Identification of ANLN as ETV6 partner gene in recurrent t(7;12)(p15;p13): a possible role of deregulated ANLN expression in leukemogenesis.
Campregher PV; Pereira WO; Lisboa B; Puga R; Helman R; Miyagi M; da Mata EH; Datoguia TS; Velloso ED; Bacal NS; Ross JS; Ali S; Miller V; Costa FF; Hamerschlak N; Santos FP
Mol Cancer; 2015 Nov; 14():197. PubMed ID: 26584717
[TBL] [Abstract][Full Text] [Related]
14. Next-generation sequencing and molecular cytogenetic characterization of ETV6-LYN fusion due to chromosomes 1, 8 and 12 rearrangement in acute myeloid leukemia.
Ma ESK; Wan TSK; Au CH; Ho DN; Ma SY; Ng MHL; Chan TL
Cancer Genet; 2017 Dec; 218-219():15-19. PubMed ID: 29153093
[TBL] [Abstract][Full Text] [Related]
15. Identification of NIPBL, a new ETV6 partner gene in t(5;12) (p13;p13)-associated acute megakaryoblastic leukemia.
de Braekeleer E; Auffret R; García JR; Padilla JM; Fletes CC; Morel F; Douet-Guilbert N; de Braekeleer M
Leuk Lymphoma; 2013 Feb; 54(2):423-4. PubMed ID: 22734863
[No Abstract] [Full Text] [Related]
16. t(5;12)(q23-31;p13) with ETV6-ACSL6 gene fusion in polycythemia vera.
Murati A; Adélaïde J; Gelsi-Boyer V; Etienne A; Rémy V; Fezoui H; Sainty D; Xerri L; Vey N; Olschwang S; Birnbaum D; Chaffanet M; Mozziconacci MJ
Leukemia; 2006 Jun; 20(6):1175-8. PubMed ID: 16572202
[No Abstract] [Full Text] [Related]
17. ETV6-NCOA2: a novel fusion gene in acute leukemia associated with coexpression of T-lymphoid and myeloid markers and frequent NOTCH1 mutations.
Strehl S; Nebral K; König M; Harbott J; Strobl H; Ratei R; Struski S; Bielorai B; Lessard M; Zimmermann M; Haas OA; Izraeli S
Clin Cancer Res; 2008 Feb; 14(4):977-83. PubMed ID: 18281529
[TBL] [Abstract][Full Text] [Related]
18. t(10; 12) (q24; p13) as the sole abnormality in a case with refractory acute myeloid leukemia: The first case report and literature review.
Lu G; Gurevich I; Vo BT; Chen SS
Beijing Da Xue Xue Bao Yi Xue Ban; 2009 Aug; 41(4):480-3. PubMed ID: 19727243
[TBL] [Abstract][Full Text] [Related]
19. Translocation t(5;18)(q35;q21) as a rare nonrandom abnormality in acute myeloid leukemia.
Daraki A; Bourantas LK; Manola KN
Cytogenet Genome Res; 2013; 139(4):289-94. PubMed ID: 23548668
[TBL] [Abstract][Full Text] [Related]
20. FLT3 is fused to ETV6 in a myeloproliferative disorder with hypereosinophilia and a t(12;13)(p13;q12) translocation.
Vu HA; Xinh PT; Masuda M; Motoji T; Toyoda A; Sakaki Y; Tokunaga K; Sato Y
Leukemia; 2006 Aug; 20(8):1414-21. PubMed ID: 16761019
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]